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Amlodipine Besylate - 55154-6229-9 - (amlodipine besylate)

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Drug Information of Amlodipine Besylate

Product NDC: 55154-6229
Proprietary Name: Amlodipine Besylate
Non Proprietary Name: amlodipine besylate
Active Ingredient(s): 10    mg/1 & nbsp;   amlodipine besylate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Amlodipine Besylate

Product NDC: 55154-6229
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076418
Marketing Category: ANDA
Start Marketing Date: 20100104

Package Information of Amlodipine Besylate

Package NDC: 55154-6229-9
Package Description: 6 BLISTER PACK in 1 CARTON (55154-6229-9) > 5 TABLET in 1 BLISTER PACK

NDC Information of Amlodipine Besylate

NDC Code 55154-6229-9
Proprietary Name Amlodipine Besylate
Package Description 6 BLISTER PACK in 1 CARTON (55154-6229-9) > 5 TABLET in 1 BLISTER PACK
Product NDC 55154-6229
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amlodipine besylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100104
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name AMLODIPINE BESYLATE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Complete Information of Amlodipine Besylate


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